关键词: MYC angiosarcoma appropriate use criteria atypical vascular lesions fluorescence in situ hybridization immunohistochemistry

Mesh : Aged Aged, 80 and over Breast Neoplasms / diagnosis metabolism pathology radiotherapy Female Gene Amplification / genetics Hemangiosarcoma / diagnosis genetics metabolism mortality pathology Humans Immunohistochemistry / methods In Situ Hybridization, Fluorescence / methods Lymphedema / complications metabolism pathology Neoplasms, Radiation-Induced / diagnosis metabolism pathology Prognosis Proto-Oncogene Proteins c-myc / genetics Retrospective Studies Sensitivity and Specificity Skin Neoplasms / genetics pathology

来  源:   DOI:10.1111/cup.13912   PDF(Sci-hub)

Abstract:
BACKGROUND: Secondary angiosarcoma (AS) most commonly follows breast cancer and includes postirradiation AS (PRAS) and lymphedema-associated AS. The frequent amplification of MYC (8q24.21) in secondary AS and the rising incidence of PRAS and atypical vascular lesions (AVLs) have prompted interest in the diagnostic and prognostic utility of MYC in AS.
METHODS: Retrospective series with ≥2 cases of cutaneous AS and describing the use of fluorescence in situ hybridization (FISH) for MYC amplification or immunohistochemistry (IHC) for MYC overexpression were included.
RESULTS: Sixteen studies met inclusion criteria. Overall, 93% of cases evaluated by FISH and IHC were concordant. The sensitivity of FISH in primary AS was only 6.8%, and protein overexpression occurred without amplification in sun-damaged skin. FISH and IHC were over 78% sensitive in secondary AS but negative in over 98% of AVLs. MYC amplification and FLT4 coamplification were associated with shorter overall survival in secondary AS.
CONCLUSIONS: FISH for MYC amplification and IHC for MYC overexpression are useful in distinguishing PRAS from AVLs and may also have prognostic value in secondary AS. In contrast, these methods have little diagnostic or prognostic value in primary AS and should not be used to distinguish primary AS from benign vascular neoplasms.
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